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线性分子式:
(O=)C5H6(CH2CH=CHC2H5)CH2CO2CH3
化学文摘社编号:
分子量:
224.30
FEMA Number:
3410
Council of Europe no.:
10821
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.521
EC Number:
254-705-5
NACRES:
NA.21
MDL number:
Organoleptic:
fresh; green; jasmine; floral; fruity; sweet
Grade:
FG
Fragrance grade
Halal
Kosher
Fragrance grade
Halal
Kosher
Biological source:
synthetic
Agency:
follows IFRA guidelines
Food allergen:
no known allergens
产品名称
茉莉酸甲酯, ≥98%, stabilized, FG
SMILES string
CC\C=C\CC1C(CCC1=O)CC(=O)OC
InChI
1S/C13H20O3/c1-3-4-5-6-11-10(7-8-12(11)14)9-13(15)16-2/h4-5,10-11H,3,6-9H2,1-2H3/b5-4+
InChI key
GEWDNTWNSAZUDX-SNAWJCMRSA-N
biological source
synthetic
grade
FG
Fragrance grade
Halal
Kosher
agency
follows IFRA guidelines
reg. compliance
EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110
assay
≥98%
contains
synthetic α-tocopherol as stabilizer
refractive index
n20/D 1.474 (lit.)
bp
110 °C/0.2 mmHg (lit.)
density
1.03 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
fragrance allergen
no known allergens
organoleptic
fresh; green; jasmine; floral; fruity; sweet
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Application
可能的应用(风味): 有许多风味用途,包括李子,桃子,杏子和 tutti-frutti。
General description
茉莉酸甲酯是一种植物生长调节剂,主要用于增强部分果蔬的香气品质。
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
>235.4 °F - closed cup
flash_point_c
> 113 °C - closed cup
Xiaolong Hao et al.
Biotechnology and applied biochemistry, 62(1), 24-31 (2014-05-02)
Tanshinone is a group of active diterpenes, which are widely used in the treatment of cardiovascular disease. In this study, methyl jasmonate (MJ) and salicylic acid (SA) were used to investigate their effects on tanshinone accumulation and biosynthetic gene expression
Aroma changes of black tea prepared from methyl jasmonate treated tea plants.
Shi J, et al.
Journal of Zhejiang University. Science. B, 15(4), 313-313 (2014)
Arabidopsis mutants selected for resistance to the phytotoxin coronatine are male sterile, insensitive to methyl jasmonate, and resistant to a bacterial pathogen.
Feys BJ, et al.
Plant Cell, 6(5), 751-759 (1994)
Qiumei Liao et al.
IET nanobiotechnology, 9(1), 35-42 (2015-02-05)
The fluorescence labelling of plant hormone binding sites is an important analytical technique in research on the molecular mechanisms of plant hormone activities. The authors synthesised a jasmonic acid (JA)-conjugated ZnS:Mn quantum dot (QD) probe, with a cubic structure and
Bjørn Dueholm et al.
BMC evolutionary biology, 15, 122-122 (2015-06-27)
Large proliferations of cytochrome P450 encoding genes resulting from gene duplications can be termed as 'blooms', providing genetic material for the genesis and evolution of biosynthetic pathways. Furanocoumarins are allelochemicals produced by many of the species in Apiaceaous plants belonging
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